Complement C4 Universal Kit

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1 Order references Reagents CONT C4TUR-B00 Universal kit 1 x 50 ml R1 + 1 x 5 ml R2 C4TUR-00 Universal kit 2 x 50 ml R1 + 1 x 15 ml R2 C4TUR-C00 Universal kit 1 x 12 ml R1 + 1 x 2 ml R2 Other necessary products MPREK-000 Multiparametric Calibrators Kit (5 Levels) 5 x 1 ml MPRE-001 Multiparametric igh Calibrator 1 x 1 ml MPRE-005 Multiparametric igh Calibrator 1 x 5 ml MPCOS-002 Multiparametric Low Control 1 x 2 ml MPCON-002 Multiparametric Medium Control 1 x 2 ml MPCOX-002 Multiparametric igh control 1 x 2 ml Field of application - Purpose In vitro diagnostic reagent for the quantitative determination of complement C4 in samples of human origin by immunoturbidimetry on photometric systems. Medical benefit - Scientific validity Complement C4 is a protein with a molecular mass of 206 kda. The synthesis of complement C4 takes place mostly in the hepatic parenchyma, but a part is synthesised by monocytes or other tissues. Complement C4 is the enzyme of activation of complement C3 and C5. The complement C4 concentration can increase slightly following an acute inflammatory phase. A decrease in complement C4 concentration can be caused genetically, by hereditary angio-oedema, by autoimmune haemolytic anaemia, or autoimmune nephritis. Method principle The complement C4 contained in the sample to assay reacts specifically with anti-human complement C4 antiserum and the turbidity induced by the formation of the antigen-antibody immune complex is measured at 340 nm and 700 nm. The measured turbidity is proportional to the complement C4 concentration contained in the sample. Warning and precautions - For in vitro diagnostic use only. - Must be handled by qualified personnel under the responsibility of a biologist. - The human-origin products have been screened and found negative for IV 1 and 2 antibodies, CV antibodies and BAg, but they must nevertheless be handled as potentially infectious products. - These products contain sodium azide. Products containing sodium azide must be handled with care: avoid ingestion and contact with the skin or mucous membranes. - Sodium azide becomes explosive on contact with heavy metals such as copper or lead. 1/5

2 Samples Collection conditions Collect specimens using standard laboratory techniques; use only suitable procedures, tubes or collection containers. Sample type Fresh serum and plasma (EDTA). Storage and stability of specimens Temperature - 20 C 4-8 C C Stability 3 months 8 days 2 days This information comes from data originating from Tietz Clinical Guide to Laboratory Tests and from WO. Reagents Composition and concentrations/storage Active ingredients: Reagent R1: none. Reagent R2: anti-human complement C4 goat antiserum (titer ± 11 mg/ml). Other ingredients: Reagent R1: buffer, polymer, inorganic salt and preservative. Reagent R2: buffer, inorganic salt and preservative. Storage temperature: Reagent R1: 2-25 C. Reagent R2: 2-8 C Preparation Ready to use. Storage and stability Reagents are stable until the expiration date printed on the packaging (months passed), under the following recommended storage and handling conditions: - Unopened vial stored at temperature indicated on packaging. - Opened vial: closed immediately after use or placed on closed analyser intended for this purpose, not contaminated by handling and stored at the temperature indicated on the packaging. Note: - Do not freeze the reagents. - Nanoparticle-based reagents can settle over time. It may be necessary to delicately mix by repeated turning. Other materials required Usual laboratory equipment including an analytical system equipped with a photometric detector. Calibration Calibration The calibration curve is performed by using the calibration kit indicated in the Order references section. The zero point of the calibration curve is performed with physiological saline solution. 2/5

3 Traceability The method has been standardised with a benchmark method traceable to the international standard as described in the associated calibrators data sheet (see the Order references section). Calibrate the method when the reagent batch number changes or in case of change in performance (contact the manufacturer if the changes persist) or if quality control requires it. Quality control The frequency of controls and the confidence limits must be adapted to the laboratory requirements. The results must be within the defined confidence limits. Each laboratory shall establish corrective measures to be taken if results fall outside the defined limits. Comply with current legislation in the country and local guidelines relating to quality control. The calibration curve and its stability can be validated using the control materials indicated in the Order references section. Reference values Adults (20-60 years) Reference values 0,1-0,4 g/l International units: g/l Conventional units: mg/dl This information coming from data originating from Clinical guide to laboratory tests. Each laboratory must check the validity of its values and if necessary establish its own reference values, depending on the population examined. Analytical performances The analytical performance data below are given as an indication. The results obtained in the laboratory may differ from these. The analytical performances were determined following the indications of the Guide technique d accréditation de vérification (Portée A)/validation (Portée B) des méthodes en biologie médicale ; document S GTA 04 Révision 01. Measurement range 0,002-0,825 g/l The measurement range is bounded by the quantification and linearity limits. Samples having a concentration greater than the upper limit must be diluted. Limit of detection 0,001 g/l It is the smallest signal expressed as a quantity or concentration that can be distinguished with a given probability from a reagent blank performed in the same conditions. The evaluation of the limit of detection is based on the statistical analysis of the observed signal differences between the blanks and samples. Interferences (Analytical specificity) There is no known cross-reactivity of the antiserum cited or the antibodies used. The abnormally coloured and particle-containing samples can cause, depending on the analytical system, assay errors. These samples must be clarified chemically or physically before their assay. Precision The precision is evaluated using the repeatability (CV within-run) and reproducibility (CV within-calibration). 3/5

4 Level 1 Level 2 Level 3 Level 4 Repeatability (n=30) Reproducibility (n=30) Average (g/l) CV (%) Average (g/l) CV (%) 0,14 0,77 0,13 3,48 0,32 0,76 0,32 2,52 0,46 0,64 0,47 2,08 0,38 0,86 0,37 1,08 Trueness - Accuracy Trueness, quantified by the bias, is estimated by comparing the mean obtained in the intermediate precision study, based on internal quality control samples, with the expected target value equated to the true value of the tested sample. Accuracy is defined as the closeness of agreement between a measured value and a true value of a measurand (quantity to be measured). DiAgam allows a bias of 5% compared to the international standard or compared to a reference method traceable to the international standard when it exists. Limitations of the method The results of this test should always be interpreted in relation to the patient s medical history, clinical signs and other findings. Prozone By limiting the linearity to the value of the upper limit of the measurement range, no excess antigen effect was observed for samples with a concentration up to 32,8 g/l. Matrix effect The inter-laboratory control samples and controls can yield different results from those obtained with other assay methods because of a matrix effect. In this case, an analysis of the results according to specific target values of the method utilised may be necessary. If in doubt, contact the manufacturer. Utilisation procedure If the application corresponding to the assay is not installed on your analyzer, please contact DiAgam. Indeed CE validated applications are available from the manufacturer. For a detailed description on how run an assay, please refer to the operating instructions for your system. Literature 1. Tietz Textbook of Clinical chemistry and molecular Diagnostics, fourth edition, edited by Carl A. Burtis, Edward R. Ashwood, David E. Bruns, Use of Anticoagulants in Diagnostic Laboratory Investigations & Stability of blood, plasma and serum samples. Publication WO/DIL/LAB/99.1 Rev. 2. Jan Clinical guide to laboratory tests, second edition, edited by Norbert W. Tietz, CLSI. Procedures for the Collection of Diagnostic Blood Specimens by Venipuncture; Approved Standard-Sixth Edition. CLSI document 3-A6 (ISBN ). CLSI, 940 West Valley Road, Suite 1400, Wayne, PA USA; NCCLS. Procedures and Devices for the Collection of Diagnostic Capillary Blood Specimens; Approved Standard-Fifth Edition. NCCLS document 4-A5 [ISBN ]. CLSI, 940 West Valley Road, Suite 1400, Wayne, PA USA, /5

5 Symbols legend The following symbols may appear on the packaging and the label: Batch code Use until Buffer Calibrator Manufacturer igh In vitro diagnostic medical device Moderate Temperature (Storage at) Low Catalogue reference Read the usage instructions Reagent Kit Content Antibody or Antisera 4 levels 5 levels 6 levels Control This product meets the requirements of European Directive 98/79 EC concerning in vitro diagnostic medical devices DiAgam Belgium: Rue du Parc Industriel 40, 7822 Ghislenghien, Belgium DiAgam eadquarters Distributed by Avenue Louis Lepoutre 70, 1050 Bruxelles, Belgique DiAgam France: Boulevard de la Liberté 130, Lille, France All product names, registered trademarks, company names in this document remain the property of their respective owners. 5/5

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